Description

Book Synopsis
The formulation and the technological advancements in RNA biology, chemistry, stability, and encapsulated delivery systems that have enabled the development of fully synthetic mRNA vaccines are discussed in this volume. The applications of the mRNA technology is covered, focusing on infectious diseases but also touching on other indications, such as immunotherapies and molecular therapies. Potent and long-lasting immune responses observed in animal models, encouraging data from early human clinical studies, together with the success of two mRNA-based COVID-19 vaccines support the use of mRNA-based vaccination as an attractive alternative to conventional vaccine approaches. Consequently, the development progress of the technology, particularly on production, capabilities, and clinical development is reviewed. Topics on safety, regulatory issues, and possible challenges to the mRNA vaccination approach round off this book. Thanks to their high potency, the prospect for generic, low-cost manufacturing processes, and entirely synthetic nature, the future for mRNA vaccines is highly promising. Importantly, mRNA vaccines have the potential to minimize the time between pathogen identification and vaccine release with a huge impact on public health.

As the mRNA-based vaccination technology has been progressing rapidly, the book is intended to be an end-to-end review series, covering everything from basic RNA biology and preclinical studies to the manufacturing strategy, clinical development and regulatory approval. It provides established RNA researchers and developers with updates on the latest advancements in the field and allows for a quick but comprehensive overview of this transformative technology, its application, and future potential.



Table of Contents

Foreword - RNA technology overview

Dong Yu (dong.x.yu@gsk.com) (GSK) & Frank Bähner (Frank.Baehner@curevac.com) (CureVac) – confirmed

Conventional mRNA-based technology & mode of action

Benjamin Petsch (benjamin.petsch@curevac.com) (CureVac) – confirmed

Self-amplifying RNA-based technology & mode of action

Jeffrey Ulmer (jeffrey.b.ulmer@gsk.com)/Dong Yu (dong.x.yu@gsk.com) (GSK) – confirmed

Delivery and formulation technologies

Yizhou Dong (dong.525@osu.edu) (Ohio State) – confirmed

RNA for infectious disease applications

Drew Weissman (dreww@pennmedicine.upenn.edu) (U Penn) – confirmed

RNA for other indications (immunotherapies/oncology, molecular therapies - a potential topic)

Tim Wagenaar (Timothy.Wagenaar@sanofi.com) (Sanofi) – tentatively confirmed, likely working with Biotech; Backup - Katalin Karikó (BioNTech)

Production and capabilities

Heinrich Haas (Heinrich.Haas@biontech.de) (Biontech) – waiting for response; Backup - Juan Andres (Moderna)

Clinical development

Tal Zaks (Tal.Zaks@modernatx.com) (Moderna) – tentatively confirmed; Backup - Anna Collén (AstraZeneca)

Other considerations (e.g., safety, regulatory issues, challenges)

Mark Tracy (mark@tracybioconsulting.com) (Tracy Bioconsulting) – waiting for response

mRNA Vaccines

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    A Hardback by Dong Yu, Benjamin Petsch

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      Publisher: Springer International Publishing AG
      Publication Date: Publication Date: 04/01/2023
      ISBN13: 9783031180699, 978-3031180699
      ISBN10: 3031180690

      Description

      Book Synopsis
      The formulation and the technological advancements in RNA biology, chemistry, stability, and encapsulated delivery systems that have enabled the development of fully synthetic mRNA vaccines are discussed in this volume. The applications of the mRNA technology is covered, focusing on infectious diseases but also touching on other indications, such as immunotherapies and molecular therapies. Potent and long-lasting immune responses observed in animal models, encouraging data from early human clinical studies, together with the success of two mRNA-based COVID-19 vaccines support the use of mRNA-based vaccination as an attractive alternative to conventional vaccine approaches. Consequently, the development progress of the technology, particularly on production, capabilities, and clinical development is reviewed. Topics on safety, regulatory issues, and possible challenges to the mRNA vaccination approach round off this book. Thanks to their high potency, the prospect for generic, low-cost manufacturing processes, and entirely synthetic nature, the future for mRNA vaccines is highly promising. Importantly, mRNA vaccines have the potential to minimize the time between pathogen identification and vaccine release with a huge impact on public health.

      As the mRNA-based vaccination technology has been progressing rapidly, the book is intended to be an end-to-end review series, covering everything from basic RNA biology and preclinical studies to the manufacturing strategy, clinical development and regulatory approval. It provides established RNA researchers and developers with updates on the latest advancements in the field and allows for a quick but comprehensive overview of this transformative technology, its application, and future potential.



      Table of Contents

      Foreword - RNA technology overview

      Dong Yu (dong.x.yu@gsk.com) (GSK) & Frank Bähner (Frank.Baehner@curevac.com) (CureVac) – confirmed

      Conventional mRNA-based technology & mode of action

      Benjamin Petsch (benjamin.petsch@curevac.com) (CureVac) – confirmed

      Self-amplifying RNA-based technology & mode of action

      Jeffrey Ulmer (jeffrey.b.ulmer@gsk.com)/Dong Yu (dong.x.yu@gsk.com) (GSK) – confirmed

      Delivery and formulation technologies

      Yizhou Dong (dong.525@osu.edu) (Ohio State) – confirmed

      RNA for infectious disease applications

      Drew Weissman (dreww@pennmedicine.upenn.edu) (U Penn) – confirmed

      RNA for other indications (immunotherapies/oncology, molecular therapies - a potential topic)

      Tim Wagenaar (Timothy.Wagenaar@sanofi.com) (Sanofi) – tentatively confirmed, likely working with Biotech; Backup - Katalin Karikó (BioNTech)

      Production and capabilities

      Heinrich Haas (Heinrich.Haas@biontech.de) (Biontech) – waiting for response; Backup - Juan Andres (Moderna)

      Clinical development

      Tal Zaks (Tal.Zaks@modernatx.com) (Moderna) – tentatively confirmed; Backup - Anna Collén (AstraZeneca)

      Other considerations (e.g., safety, regulatory issues, challenges)

      Mark Tracy (mark@tracybioconsulting.com) (Tracy Bioconsulting) – waiting for response

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